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Matrix metalloproteinase 3 messenger RNA 3'-untranslated region (MMP3 mRNA 3'-UTR) (MMP3 mRNA 3'-UTR)

Target
MMP3 mRNA 3'-UTR
Molecular classification
Messenger RNA, RNA regulatory element
01

Overview

The Matrix metalloproteinase 3 (MMP3) mRNA 3'-untranslated region (3'-UTR) is a critical regulatory segment of the MMP3 transcript that governs the enzyme's expression through post-transcriptional mechanisms (PMID: 24603414). MMP3, also known as stromelysin-1, is a proteoglycanase capable of degrading various components of the extracellular matrix, including collagen types II, IV, IX, and X, as well as laminin and fibronectin (UniProt P08281). The 3'-UTR contains specific binding sites for microRNAs (miRNAs) such as miR-140 and miR-519d, which modulate mRNA stability and translational efficiency (PMID: 30106614). Dysregulation of MMP3 expression, often mediated by changes in 3'-UTR interactions, is a hallmark of degenerative joint diseases like osteoarthritis and rheumatoid arthritis, where excessive MMP3 leads to cartilage destruction (PMID: 21163941). Furthermore, MMP3 is implicated in cancer progression, facilitating tumor cell invasion and metastasis by degrading the basement membrane. Therapeutic strategies targeting the MMP3 mRNA 3'-UTR, such as miRNA mimics or antisense oligonucleotides, aim to reduce pathological MMP3 levels by promoting transcript degradation or inhibiting translation, thereby preserving tissue integrity in inflammatory and oncological contexts.

Other names
Stromelysin-1 mRNA 3'-UTRMMP-3 mRNA 3'-UTRMatrix metallopeptidase 3 mRNA 3'-UTRMMP3 3'-untranslated region
02

Mechanism of action

MicroRNA-mediated gene silencing and antisense-mediated mRNA degradation or translational repression targeting the 3'-UTR to reduce MMP3 protein expression.

03

Biological functions

Post-transcriptional regulationmRNA stability regulationTranslation regulationMicroRNA mediated gene silencing
04

Disease associations

OsteoarthritisRheumatoid arthritisCancer metastasisIntervertebral disc degenerationAtherosclerosis
05

Safety considerations

Off-target RNA binding due to sequence homology with other MMP family membersInnate immune activation by synthetic oligonucleotidesPotential for musculoskeletal syndrome if broad MMP inhibition occursDelivery challenges to avascular tissues like articular cartilage
06

Interacting drugs

miR-140 mimics (experimental)

3 more in the full profile.

07

Biomarkers

MMP3 protein levelsMMP3 mRNA expression levelsC-terminal telopeptide of type II collagen (CTX-II)

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